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Olmesartan Medoxomil

NDC 65862-741 · Aurobindo Pharma Limited

Generic nameOlmesartan Medoxomil
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)OLMESARTAN MEDOXOMIL
Strength5 mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
Marketing categoryANDA

Packages

65862-741-01 — 100 TABLET, FILM COATED in 1 BOTTLE (65862-741-01)

65862-741-05 — 500 TABLET, FILM COATED in 1 BOTTLE (65862-741-05)

65862-741-30 — 30 TABLET, FILM COATED in 1 BOTTLE (65862-741-30)

65862-741-90 — 90 TABLET, FILM COATED in 1 BOTTLE (65862-741-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63629-2241 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 63629-4307 — Olmesartan Medoxomil and Hydrochlorothiazide, 63629-8522 — olmesartan medoxomil, 63629-8523 — olmesartan medoxomil, 63629-8524 — olmesartan medoxomil, 63629-8525 — olmesartan medoxomil, 63629-9426 — olmesartan medoxomil, 64980-602 — olmesartan medoxomil, 64980-603 — olmesartan medoxomil, 64980-665 — olmesartan medoxomil, 65862-742 — Olmesartan Medoxomil, 65862-743 — Olmesartan Medoxomil, 65862-779 — Olmesartan Medoxomil and Hydrochlorothiazide, 65862-780 — Olmesartan Medoxomil and Hydrochlorothiazide, 65862-781 — Olmesartan Medoxomil and Hydrochlorothiazide, 65862-854 — Amlodipine and Olmesartan Medoxomil, 65862-855 — Amlodipine and Olmesartan Medoxomil, 65862-856 — Amlodipine and Olmesartan Medoxomil, 65862-857 — Amlodipine and Olmesartan Medoxomil, 67877-445 — Olmesartan Medoxomil, +281 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.